Johnson Linda K, Widi Antin Yn, Rowarth Serrin, Baxter Alan G
College of Public Health, Medical and Veterinary Science, James Cook University, Townsville, Queensland, Australia.
College of Public Health, Medical and Veterinary Science, James Cook University, Townsville, Queensland, Australia; Faculty of Veterinary Medicine, Nusa Cendana University, Kupang, East Nusa Tenggara, Indonesia.
Comp Med. 2015 Apr;65(2):123-6.
Here we describe the gross and microscopic findings of naturally occurring, β-hemolytic Escherichia coli peritonitis in B6.129-Myd88(tm1Aki) male and female mice. Over approximately 5 mo, 10 homozygous mutant mice deficient in myeloid differentiation factor 88 (C57BL/6 strain; male and female) that had not been used in research protocols developed rapid-onset abdominal swelling associated with copious viscous ascites. Each mouse developed an anterior peritonitis, primarily involving the parietal peritoneum and the visceral surface of the spleen, liver, diaphragm, and stomach. Inflammation was confined to the organ surfaces, with no indication of septicemia or grossly apparent gastrointestinal perforation or other tissue compromise that would initiate peritonitis. Peritonitis was likely attributable to compromised antibacterial innate immunity; cohoused, similarly immunodeficient littermates did not develop similar clinical signs. An unusual finding in all cases was mesothelial cell hyperplasia and hypertrophy. Although the underlying innate immune deficiency accounts for much of the observed pathology, the remarkable mesothelial cell morphology and the episodic nature of the peritonitis in some littermates and not others remain unexplained.
在此,我们描述了B6.129-Myd88(tm1Aki)雄性和雌性小鼠自然发生的β-溶血性大肠杆菌腹膜炎的大体和微观发现。在大约5个月的时间里,10只未用于研究方案的髓样分化因子88缺陷纯合突变小鼠(C57BL/6品系;雄性和雌性)迅速出现腹部肿胀,并伴有大量粘性腹水。每只小鼠都发生了前腹膜炎,主要累及壁层腹膜以及脾脏、肝脏、膈肌和胃的脏面。炎症局限于器官表面,没有败血症迹象,也没有明显的胃肠道穿孔或其他会引发腹膜炎的组织损伤。腹膜炎可能归因于抗菌天然免疫受损;同笼饲养的、免疫缺陷程度相似的同窝小鼠未出现类似的临床症状。所有病例中的一个不寻常发现是间皮细胞增生和肥大。虽然潜在的天然免疫缺陷是观察到的大部分病理现象的原因,但间皮细胞显著的形态以及某些同窝小鼠发生腹膜炎而其他同窝小鼠未发生的间歇性特征仍无法解释。